Table 3. Safety endpoint.
Topiroxostat (n = 70) | % | Allopurinol (n = 70) | % | P Value | |
---|---|---|---|---|---|
Adverse events, n (%) | 21 | 30.0 | 14 | 20.0 | 0.17 |
Serious adverse events, n (%) | 6 | 8.6 | 5 | 7.1 | 0.75 |
Unknown adverse events, n (%) | 5 | 7.1 | 4 | 5.7 | – |
Probably related adverse events, n (%) | 1 | 1.4 | 0 | 0.0 | – |
Serious adverse events necessitating withdrawal from the study, n (%) | 1 | 1.4 | 2 | 2.9 | – |
Serious cardiovascular adverse events, n (%) | 3 | 4.3 | 3 | 4.3 | – |
Gouty arthritis, n (%) | 1 | 1.4 | 0 | 0.0 | – |
Hepatic function abnormality, n (%) | 1 | 1.4 | 1 | 1.4 | – |
Values are n (percentage of patients). P-values are for the between-groups difference by Wilcoxon rank-sum test.